Classes
DEA Class; Rx
Common Brand Names; Mononessa, Ortho Cyclen-28, Ortho Tri-Cyclen, Ortho Tri-Cyclen Lo, Estarylla, Tri-Estarylla, Tri-Lo-Estarylla, Mili, Mono-Linyah, Tri-Linyah, Previfem, Sprintec 28, TriCyclen, Tri-Lo Sprintec, Tri-Mili, Tri-Lo-Mili, Trinessa, TriNessa Lo, TriPrevifem, TriSprintec, Femynor, TriFemynor, Tri-Lo-Marzia
- Estrogens/Progestins;
- Contraceptives, Oral
Description
Combined oral contraceptive (COC) containing norgestimate, a progestin with low androgenic and negligible estrogenic effect, and ethinyl estradiol, a synthetic estrogen
Used for routine contraception in adolescent and adult premenopausal females; some products additionally used for acne in these populations
All COCs contain a boxed warning regarding the increased risk for thromboembolism in women who smoke
Indications
Indicated for routine contraception.
Contraindications
Documented hypersensitivity
Active or history of breast cancer
Arterial thromboembolic disease (stroke, myocardial infarction [MI]), thrombophlebitis, DVT/pulmonary embolism (PE), thrombogenic valvular disease
Estrogen-dependent neoplasia
Liver disease, liver tumors
Undiagnosed abnormal uterine bleeding
Uncontrolled hypertension (ie, persistent BP values >160 mm Hg systolic or >100 mg Hg diastolic)
Diabetes mellitus with vascular involvement
Jaundice with previous oral contraceptive use
Receiving hepatitis C drug combinations containing ombitasvir/paritaprevir/ritonavir, with or without dasabuvir
Women > 35 years who smoke
Cerebrovascular and/or coronary artery disease, disease, headaches with focal neurological symptoms, migraine headaches with auro or migraine headaches if >35 years of age
Adverse Effects
- Amenorrhea
- Anorexia
- Aterial thromboembolism
- Cerebral hemorrhage
- Crebral thrombosis
- Retinal thrombosis
- Breakthrough bleeding
- Change in menstrual flow
- Gallbladder disease
- Edema
- Spotting
- Weakness
- Abdominal pain
- Breast tenderness
- Cholestatic jaundice
- Deep vein thrombosis (DVT)
- Depression
- Dizziness
- Galactorrhea
- Headache
- Nausea
- Nervousness
- Somnolence
- Thrombophlebitis
- Varicose vein aggravation
- Vomiting
- Weight change
Warnings
Use caution in family history of breast cancer and or DVT/PE, current or previous depression, endometriosis, diabetes mellitus, hypertension, bone mineral density changes, renal or hepatic impairment, bone metabolic disease, systemic lupus erythematosus (SLE), conditions exacerbated by fluid retention (eg, migraine, asthma, epilepsy)
Monitor prediabetic and diabetic women on therapy; consider alternate contraceptive method for women with uncontrolled dyslipidemia
Headache: Evaluate significant change in headaches and discontinue therapy if indicated
Women with a history of hypertension or hypertension-related diseases, or renal disease should be encouraged to use another method of contraception
Discontinue if any of the following develop: Jaundice, visual problems (may cause contact lens intolerance), signs of venous thromboembolism, migraine with unusual severity, significant blood pressure increase, severe depression, increased risk of thromboembolic complications after surgery
Discontinue 4 weeks before major surgery or prolonged immobilization
Patients on warfarin or oral anticoagulants: Increase in anticoagulant dosage may be warranted
Some studies link oral contraceptive use with increased risk of breast cancer, whereas others do not; risk depends on conditions where naturally high hormone levels persist for long periods, including early-onset menstruation (age <12 years), late-onset menopause (age >55 years), first child after age 30 years, nulliparity
Increased risk of cervical cancer with oral contraceptive use, however, human papillomavirus (HPV) remains primary risk factor for this cancer
Long-term (≥5years) use of oral contraceptives may be associated with increased risk
Increased risk of liver cancer with oral contraceptive use; risk increases with duration of use
Discontinue hormonal therapy prior to starting therapy with combination drug regimen ombitasvir/paritaprevir/ritonavir, with or without dasabuvir; may restart approximately 2 weeks following completion of treatment with combination drug regimen
Chloasma associated with combination hormonal contraceptives, as well as pregnancy and sun exposure; avoid sun exposure or ultraviolet radiation during therapy
Risk of cholestasis increased with prior history of cholestasis with prior contraceptive use or previous cholestasis of pregnancy
Combination hormonal contraceptives may adversely affect lipid levels; consider alternative contraception for women with uncontrolled dyslipidemia
Retinal vascular thrombosis reported in patients receiving estrogens; discontinue medication pending examination if there is sudden partial or complete loss of vision, or a sudden onset of proptosis, diplopia, or migraine; if examination reveals papilledema or retinal vascular lesions, estrogens should be discontinued
Pregnancy and Lactation
Pregnancy category: X
Lactation: Small amounts of steroids are excreted in breast milk; estrogens may reduce quality or quantity of milk; may be prudent to use other forms of birth control until full weaning (American Academy of Pediatrics committee states that agent is compatible with nursing); not recommended
Maximum Dosage
Dependent on product used and indication for therapy.
Not indicated.
Dependent on product used and indication for therapy.
Not indicated in prepubescent females.
How supplied
Norgestimate/ethinyl estradiol
tablet, monophasic (Estarylla, Femynor, Mili, MonoNessa, Previfem, Sprintec)
- Days 1-21: 0.25mg/35mcg
- Days 22-28: Inert tablets
tablet, triphasic (Ortho Tri-Cyclen, Tri-Estarylla, TriFemynor, Tri-Mili, Trinessa, Tri-Sprintec, Tri-Previfem)
- Days 1-7: 0.18mg/35mcg
- Days 8-14: 0.215mg/35mcg
- Days 15-21: 0.25mg/35mcg
- Days 22-28: Inert tablets
tablet, triphasic (Ortho Tri-Cyclen Lo, Tri-Lo-Estarylla, Tri-Lo-Marzia, Tri-Lo-Mili)
- Days 1-7: 0.18mg/25mcg
- Days 8-14: 0.215mg/25mcg
- Days 15-21: 0.25mg/25mcg
- Days 22-28: Inert tablets